Any skeletal dysplasia in which the cause of the disease is a variation in FAM111A gene.
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osteochondrodysplasia
MONDO:0005516
diaphyseal medullary stenosis-bone malignancy syndrome
MONDO:0007205
fibular aplasia-ectrodactyly syndrome
MONDO:0007225
cerebrocostomandibular syndrome
MONDO:0007301
cleidorhizomelic syndrome
MONDO:0007341
autosomal dominant Kenny-Caffey syndrome
MONDO:0007478